FDA inspection
Goetze-Niemer Co Inc: FDA inspection ending Dec 14, 2015
FDA inspection 952168 · Voluntary Action Indicated (VAI) · Kansas City, MO
Key facts
| Inspection ID | 952168 |
|---|---|
| Firm | Goetze-Niemer Co Inc |
| FEI number | 3002177077 |
| Address | 3939 Ne 33rd Ter Ste J |
| City | Kansas City |
| State | MO |
| ZIP | 64117 |
| Country | United States |
| Fiscal year | 2016 |
| Inspection end date | Dec 14, 2015 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Human Cellular, Tissue, and Gene Therapies |
| Product type | Biologics |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 1–9 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data